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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

DIXION — Class IIa MDR by Dixion Vertrieb…

MD Atlas
Dixion Vertrieb medizinischer Geräte GmbH

EUDAMED last updated this device on May 20, 2026

DIXION

4260664650704XR

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Dixion Vertrieb medizinischer Geräte GmbH
UDI-DI code: 04260664655770
Reference / catalog number: 7209

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Manufacturer information

Organization name: Dixion Vertrieb medizinischer Geräte GmbH
SRN: DE-MF-000005423
Manufacturer status: Active

Related devices

DIXION4260664650808Y6On the market DIXION4260664651627Y7On the market DIXION4260664650404XAOn the market DIXION4260664651421XHOn the market DIXION4260664651411XEOn the market

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Jan 28, 2010	Still on market

Device identification

Trade name: DIXION
UDI-DI code: 04260664655770
Basic UDI-DI: 4260664650704XR
Reference / catalog number: 7209
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z120105SURGICAL MEDICAL ASPIRATORS

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.